The Broad Institute of MIT and Harvard, Cambridge, United States.
Department of Molecular Biology, Massachusetts General Hospital, Boston, United States.
Elife. 2021 Apr 19;10:e67310. doi: 10.7554/eLife.67310.
In this era of rising antibiotic resistance, in contrast to our increasing understanding of mechanisms that cause resistance, our understanding of mechanisms that influence the propensity to evolve resistance remains limited. Here, we identified genetic factors that facilitate the evolution of resistance to carbapenems, the antibiotic of 'last resort', in , the major carbapenem-resistant species. In clinical isolates, we found that high-level transposon insertional mutagenesis plays an important role in contributing to high-level resistance frequencies in several major and emerging carbapenem-resistant lineages. A broader spectrum of resistance-conferring mutations for select carbapenems such as ertapenem also enables higher resistance frequencies and, importantly, creates stepping-stones to achieve high-level resistance to all carbapenems. These mutational mechanisms can contribute to the evolution of resistance, in conjunction with the loss of systems that restrict horizontal resistance gene uptake, such as the CRISPR-Cas system. Given the need for greater antibiotic stewardship, these findings argue that in addition to considering the current efficacy of an antibiotic for a clinical isolate in antibiotic selection, considerations of future efficacy are also important. The genetic background of a clinical isolate and the exact antibiotic identity can and should also be considered as they are determinants of a strain's propensity to become resistant. Together, these findings thus provide a molecular framework for understanding acquisition of carbapenem resistance in with important implications for diagnosing and treating this important class of pathogens.
在抗生素耐药性日益严重的时代,我们越来越了解导致耐药性的机制,但对于影响产生耐药性倾向的机制的了解仍然有限。在这里,我们确定了有助于碳青霉烯类抗生素(抗生素的最后手段)耐药性进化的遗传因素, 是主要的碳青霉烯类耐药物种。在临床分离株中,我们发现高水平转座子插入诱变在几个主要和新兴的碳青霉烯类耐药谱系中导致高水平耐药频率方面发挥了重要作用。一些选择性碳青霉烯类药物(如厄他培南)赋予更高耐药频率的更广泛的耐药性突变也使它们能够实现对所有碳青霉烯类药物的高水平耐药性,这一点很重要。这些突变机制可以与限制水平基因转移的系统(如 CRISPR-Cas 系统)的丧失一起,有助于耐药性的进化。鉴于需要更好地管理抗生素,这些发现表明,除了考虑临床分离株中抗生素对当前疗效外,还需要考虑未来的疗效。临床分离株的遗传背景和确切的抗生素身份也可以而且应该被视为决定菌株耐药倾向的因素。总之,这些发现为理解 中碳青霉烯类耐药性的获得提供了一个分子框架,对诊断和治疗这一重要病原体类具有重要意义。